Enantiomeric composition of (3R)-(-)- and (3S)-(+)-linalool in various essential oils of Indian origin by enantioselective capillary gas chromatography-flame ionization and mass spectrometry detection methods.
Identifieur interne : 000968 ( PubMed/Corpus ); précédent : 000967; suivant : 000969Enantiomeric composition of (3R)-(-)- and (3S)-(+)-linalool in various essential oils of Indian origin by enantioselective capillary gas chromatography-flame ionization and mass spectrometry detection methods.
Auteurs : Chandan S. Chanotiya ; Anju YadavSource :
- Natural product communications [ 1934-578X ] ; 2009.
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Monoterpenes, Oils, Volatile.
- chemical , isolation & purification : Monoterpenes, Oils, Volatile.
- geographic : India.
- chemistry : Plants.
- Chromatography, Gas, Flame Ionization, Mass Spectrometry.
Abstract
Enantiomeric ratios of linalool have been determined in various authentic essential oils of Indian origin using 10% heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-beta-cyclodextrin as a chiral stationary phase. A complete enantiomeric excess (ee) for (3S)-(+)-linalool was characteristic of Lippia alba and Cinnamomum tamala leaf oils while less than 90% excess was noticed in Zanthoxylum armatum leaf, Zingiber roseum root/rhizome and Citrus sinensis leaf oils. On the contrary, an enantiomeric excess of (3R)-(-)-linalool characterizes essential oils of basil (100% for Ocimum basilicum) and bergamot mint (72 to 75% for Mentha citrata). Notably, some essential oils containing both enantiomers in equal ratios or in racemic forms are rose, geranium, lemongrass and Origanum. The enantiomeric composition studies are discussed as indicators of origin authenticity and quality of essential oil of Indian origin.
PubMed: 19476006
Links to Exploration step
pubmed:19476006Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Enantiomeric composition of (3R)-(-)- and (3S)-(+)-linalool in various essential oils of Indian origin by enantioselective capillary gas chromatography-flame ionization and mass spectrometry detection methods.</title>
<author><name sortKey="Chanotiya, Chandan S" sort="Chanotiya, Chandan S" uniqKey="Chanotiya C" first="Chandan S" last="Chanotiya">Chandan S. Chanotiya</name>
<affiliation><nlm:affiliation>Instrumentation and Central Facility, Central Institute of Medicinal and Aromatic Plants, Post CIMAP, Lucknow-226 015, India. chanotiya@gmail.com</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Yadav, Anju" sort="Yadav, Anju" uniqKey="Yadav A" first="Anju" last="Yadav">Anju Yadav</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2009">2009</date>
<idno type="RBID">pubmed:19476006</idno>
<idno type="pmid">19476006</idno>
<idno type="wicri:Area/PubMed/Corpus">000968</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Enantiomeric composition of (3R)-(-)- and (3S)-(+)-linalool in various essential oils of Indian origin by enantioselective capillary gas chromatography-flame ionization and mass spectrometry detection methods.</title>
<author><name sortKey="Chanotiya, Chandan S" sort="Chanotiya, Chandan S" uniqKey="Chanotiya C" first="Chandan S" last="Chanotiya">Chandan S. Chanotiya</name>
<affiliation><nlm:affiliation>Instrumentation and Central Facility, Central Institute of Medicinal and Aromatic Plants, Post CIMAP, Lucknow-226 015, India. chanotiya@gmail.com</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Yadav, Anju" sort="Yadav, Anju" uniqKey="Yadav A" first="Anju" last="Yadav">Anju Yadav</name>
</author>
</analytic>
<series><title level="j">Natural product communications</title>
<idno type="ISSN">1934-578X</idno>
<imprint><date when="2009" type="published">2009</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chromatography, Gas</term>
<term>Flame Ionization</term>
<term>India</term>
<term>Mass Spectrometry</term>
<term>Monoterpenes (chemistry)</term>
<term>Monoterpenes (isolation & purification)</term>
<term>Oils, Volatile (chemistry)</term>
<term>Oils, Volatile (isolation & purification)</term>
<term>Plants (chemistry)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Monoterpenes</term>
<term>Oils, Volatile</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Monoterpenes</term>
<term>Oils, Volatile</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>India</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Plants</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Chromatography, Gas</term>
<term>Flame Ionization</term>
<term>Mass Spectrometry</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Enantiomeric ratios of linalool have been determined in various authentic essential oils of Indian origin using 10% heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-beta-cyclodextrin as a chiral stationary phase. A complete enantiomeric excess (ee) for (3S)-(+)-linalool was characteristic of Lippia alba and Cinnamomum tamala leaf oils while less than 90% excess was noticed in Zanthoxylum armatum leaf, Zingiber roseum root/rhizome and Citrus sinensis leaf oils. On the contrary, an enantiomeric excess of (3R)-(-)-linalool characterizes essential oils of basil (100% for Ocimum basilicum) and bergamot mint (72 to 75% for Mentha citrata). Notably, some essential oils containing both enantiomers in equal ratios or in racemic forms are rose, geranium, lemongrass and Origanum. The enantiomeric composition studies are discussed as indicators of origin authenticity and quality of essential oil of Indian origin.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19476006</PMID>
<DateCreated><Year>2009</Year>
<Month>5</Month>
<Day>29</Day>
</DateCreated>
<DateCompleted><Year>2009</Year>
<Month>07</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised><Year>2012</Year>
<Month>11</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">1934-578X</ISSN>
<JournalIssue CitedMedium="Print"><Volume>4</Volume>
<Issue>4</Issue>
<PubDate><Year>2009</Year>
<Month>Apr</Month>
</PubDate>
</JournalIssue>
<Title>Natural product communications</Title>
<ISOAbbreviation>Nat Prod Commun</ISOAbbreviation>
</Journal>
<ArticleTitle>Enantiomeric composition of (3R)-(-)- and (3S)-(+)-linalool in various essential oils of Indian origin by enantioselective capillary gas chromatography-flame ionization and mass spectrometry detection methods.</ArticleTitle>
<Pagination><MedlinePgn>563-6</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Enantiomeric ratios of linalool have been determined in various authentic essential oils of Indian origin using 10% heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-beta-cyclodextrin as a chiral stationary phase. A complete enantiomeric excess (ee) for (3S)-(+)-linalool was characteristic of Lippia alba and Cinnamomum tamala leaf oils while less than 90% excess was noticed in Zanthoxylum armatum leaf, Zingiber roseum root/rhizome and Citrus sinensis leaf oils. On the contrary, an enantiomeric excess of (3R)-(-)-linalool characterizes essential oils of basil (100% for Ocimum basilicum) and bergamot mint (72 to 75% for Mentha citrata). Notably, some essential oils containing both enantiomers in equal ratios or in racemic forms are rose, geranium, lemongrass and Origanum. The enantiomeric composition studies are discussed as indicators of origin authenticity and quality of essential oil of Indian origin.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chanotiya</LastName>
<ForeName>Chandan S</ForeName>
<Initials>CS</Initials>
<AffiliationInfo><Affiliation>Instrumentation and Central Facility, Central Institute of Medicinal and Aromatic Plants, Post CIMAP, Lucknow-226 015, India. chanotiya@gmail.com</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Yadav</LastName>
<ForeName>Anju</ForeName>
<Initials>A</Initials>
</Author>
</AuthorList>
<Language>ENG</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Nat Prod Commun</MedlineTA>
<NlmUniqueID>101477873</NlmUniqueID>
<ISSNLinking>1555-9475</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D039821">Monoterpenes</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D009822">Oils, Volatile</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>D81QY6I88E</RegistryNumber>
<NameOfSubstance UI="C018584">linalool</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D002849" MajorTopicYN="N">Chromatography, Gas</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005410" MajorTopicYN="N">Flame Ionization</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007194" MajorTopicYN="N" Type="Geographic">India</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013058" MajorTopicYN="N">Mass Spectrometry</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D039821" MajorTopicYN="N">Monoterpenes</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009822" MajorTopicYN="N">Oils, Volatile</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010944" MajorTopicYN="N">Plants</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2009</Year>
<Month>5</Month>
<Day>30</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2009</Year>
<Month>5</Month>
<Day>30</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2009</Year>
<Month>7</Month>
<Day>21</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">19476006</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Bois/explor/OrangerV1/Data/PubMed/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000968 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd -nk 000968 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Bois |area= OrangerV1 |flux= PubMed |étape= Corpus |type= RBID |clé= pubmed:19476006 |texte= Enantiomeric composition of (3R)-(-)- and (3S)-(+)-linalool in various essential oils of Indian origin by enantioselective capillary gas chromatography-flame ionization and mass spectrometry detection methods. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i -Sk "pubmed:19476006" \ | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd \ | NlmPubMed2Wicri -a OrangerV1
This area was generated with Dilib version V0.6.25. |